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Hydrogen-rich saline reduces lung injury induced by intestinal ischemia/reperfusion in rats

  • Yan Fei Mao
  • , Xing Feng Zheng
  • , Jian Mei Cai
  • , Xin Min You
  • , Xiao Ming Deng
  • , John H. Zhang
  • , Lai Jiang
  • , Xue Jun Sun

Research output: Contribution to journalArticlepeer-review

Abstract

Objective. Hydrogen has been reported to selectively reduce the hydroxyl radical, the most cytotoxic of reactive oxygen species. In this study we investigated the effects of hydrogen-rich saline on the prevention of lung injury induced by intestinal ischemia/reperfusion (I/R) in rats. Methods. Male Sprague-Dawley rats (n = 30, 200-220 g) were divided randomly into three experimental groups: sham operated, intestinal I/R plus saline treatment (5 ml/kg, i.v.), and intestinal I/R plus hydrogen-rich saline treatment (5 ml/kg, i.v.) groups. Intestinal I/R was produced by 90 min of intestinal ischemia followed by a 4 h of reperfusion. Results. Hydrogen-rich saline treatment decreased the neutrophil infiltration, the lipid membrane peroxidation, NF-κB activation and the pro-inflammatory cytokine interleukin IL-1β and TNF-α in the lung tissues compared with those in saline-treated rat. Conclusion. Hydrogen-rich saline attenuates lung injury induced by intestinal I/R. © 2009 Elsevier Inc. All rights reserved.
Original languageEnglish
Pages (from-to)602-605
Number of pages4
JournalBiochemical and Biophysical Research Communications
Volume381
Issue number4
DOIs
StatePublished - Apr 17 2009

ASJC Scopus Subject Areas

  • Biophysics
  • Biochemistry
  • Molecular Biology
  • Cell Biology

Keywords

  • Antioxidant
  • Hydrogen-rich saline
  • Intestinal ischemia/reperfusion
  • Lung injury
  • Oxidative stress
  • Cell Membrane
  • Lung Injury/etiology
  • Neutrophils
  • Interleukin-1beta/metabolism
  • Rats
  • Male
  • Rats, Sprague-Dawley
  • Animals
  • Tumor Necrosis Factor-alpha/metabolism
  • Sodium Chloride/therapeutic use
  • Hydrogen/therapeutic use
  • Intestines/blood supply
  • Reperfusion Injury/complications
  • NF-kappa B/metabolism
  • Lipid Peroxidation

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